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| Product | Description | |
|---|---|---|
| TGR5 Receptor Agonist (3-(2-Chlorophenyl)-N-(4-chlorophenyl)-N,5-dimethylisoxazole-4-carboxamide) | Cell-permeable, small molecule agonist of TGR5 G-protein coupled receptor. This agonist has shown to increase glucagon like peptide-1 (GLP-1) secretion from primary intestinal cells. Group: Biochemicals. Alternative Names: 3-(2-Chlorophenyl)-N-(4-chlorophenyl)-N,5-dimethylisoxazole-4-carboxamide. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. |  Worldwide |
| TGR5 Receptor Agonist, Cpd23g ( (4-cyclopropyl-3, 4-dihydroquinoxalin-1 (2H) -yl) (4- (2, 5-dimethylphenoxy) pyridin-3-yl) methanone, Bile Acid Receptor GPBAR-1 Agonist, Bile Acid Receptor Agonist, G Protein-coupled Bile Acid Receptor 1 Agonist) | A cell-permeable, orally available, phenoxypyrimidine carboxamide derivative that acts as a highly potent and selective agonist of Protein coupled receptor TGR5 (EC50 = 720 pM and 6.2nM for human and mouse TGR5, respectively). Does not exhibit any significant affinity towards other related targets such as GPR40, GPR119, and GPR120. Shown to increase glucagon-like peptide-1 (GLP-1) secretion in a dose-dependent manner and significantly reduce blood glucose levels in db/db mice following a single oral dose (50mg/kg). Exhibits desirable pharmacokinetic properties in rodent models (t½ = 1.5h, Cmax = 56ng/ml; and AUC = 147ng.h/ml following an oral dose of 5mg/kg). Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| TGX-115, PI3K Inhibitor (8-(2-Methylphenoxy)-2-(4-morphonilyl)-4(1H)-quinolinone) | Cell-permeable. A potent and selective inhibitor of PI 3-K isoforms p110b/p110e (IC?? p110b=0.13uM, p110e=0.63uM). Group: Biochemicals. Grades: Highly Purified. CAS No. 351071-62-0. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| TGX-221 | TGX-221 is a potent, selective, and cell membrane permeable inhibitor of the PI3K p110β catalytic subunit, used for cancer treatment. Uses: Scientific research. Group: Signaling pathways. CAS No. 663619-89-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10114. |  |
| TGX-221, PI3K Inhibitor (±)-7-Methyl-2-(morpholin-4-yl)-9-(1-phenylaminoethyl)-pyrido[1,2-a]-pyrimidin-4-one) | Cell-permeable. A potent, selective and ATP-competitive inhibitor of PI 3-kinase b (IC?? = 5nM for p110b). Inhibits other PI3K isoforms at higher concentrations (IC?? = 0.1uM for p110e, 5uM for p110a, and 3.5uM for p110g). Group: Biochemicals. Grades: Highly Purified. CAS No. 663619-89-4. Pack Sizes: 1mg, 5mg. US Biological Life Sciences. | Worldwide |
| TH1020 | TH1020 is a potent and selective toll-like receptor 5 (TLR5)/flagellin complex antagonist with an IC50 of 0.85 ?M. TH1020 inhbits flagellin-induced TLR5 signaling. TH1020 is inactive against TLR2, TLR3, TLR4, TLR7 and TLR8[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1841460-82-9. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-116961. | |
| TH1020 | ?95% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| TH10785 | TH10785 is a DNA glycosylase 1 (OGG1) activator, TH10785 can interact with the phenylalanine-319 and glycine-42 amino acids of OGG1 and increase the enzyme activity, generates ?, ?-lyase enzymatic function. TH10785 can control the catalytic activity mediated by a nitrogen base within its molecular structure. TH10785 can be used for the research of various diseases and aging connected with DNA oxidative lesions[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1002801-51-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-147313. | |
| TH1217 | TH1217 (ZINC1775962367) is a potent and selective dCTPase pyrophosphatase 1 (dCTPase) inhibitor, with an IC50 of 47 nM. TH1217 enhances the cytotoxic effect of cytidine analogues in leukemia cells. TH1217 also could modulate SARS-Cov-2 interactors, so it shows activity of against COVID-19[1][2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ZINC1775962367. CAS No. 1862212-48-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-135909. | |
| TH1834 | TH1834 is a specific Tip60 (KAT5) histone acetyltransferase (HAT) inhibitor. TH1834 induces apoptosis and increases DNA damage in breast cancer. TH1834 does not affect the activity of related histone acetyltransferase MOF. Anticancer activity[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2108830-08-4. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-123604. | |
| TH257 | TH257 is a Potent and selective allosteric LIMK 1/2 inhibitor. Uses: Designed for use in research and industrial production. Additional or Alternative Names: TH257; TH-257; TH 257. Product Category: Inhibitors. Appearance: Solid powder. CAS No. 2244678-29-1. Molecular formula: C24H26N2O3S. Mole weight: 422.54. Purity: >98%. IUPACName: N-Butyl-4-[(phenylamino)sulfonyl]-N-(phenylmethyl)benzamide. Canonical SMILES: O=C(N(CCCC)CC1=CC=CC=C1)C2=CC=C(S(=O)(NC3=CC=CC=C3)=O)C=C2. Product ID: ACM2244678291. Alfa Chemistry ISO 9001:2015 Certified. Categories: TH 257 (MN). |  |
| TH-257 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| TH-263 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| TH287 hydrochloride | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| TH5427 | TH5427 is a promising, targeted inhibitor that can be used to further study NUDT5 activity and ADP-ribose metabolism. TH5427, blocks progestin-dependent, PAR-derived nuclear ATP synthesis and subsequent chromatin remodeling, gene regulation and proliferation in breast cancer cells. NUDT5 is recently identified as a rheostat of hormone-dependent gene regulation and proliferation in breast cancer cells [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2253744-56-6. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-125209. | |
| TH5487 | TH5487 is a potent 8-oxoguanine DNA glycosylase 1 (OGG1) inhibitor with an IC50 of 342 nM. TH5487 stops OGG1 from recognizing its DNA substrate, inhibits DNA repair and modifies OGG1 chromatin dynamics, which results in the inhibition of proinflammatory pathway genes[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2304947-71-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-125276. | |
| TH588 | TH588 is a potent inhibitor of human 7,8-Dihydro-8-oxoguaninetriphosphatase MTH1 (NUDT1) with an IC50 value of 5 nM and good metabolic stability. Cancers have dysfunctional redox regulation resulting in reactive oxygen species production, damaging both DNA and free dNTPs. The MTH1 protein sanitizes oxidized dNTP pools to prevent incorporation of damaged bases during DNA replication. TH588 a first-in-class nudix hydrolase family inhibitor that potently and selectively engages and inhibits the MTH1 protein in cells. Protein co-crystal structures demonstrate that the inhibitor binds in the active site of MTH1. Uses: Designed for use in research and industrial production. Additional or Alternative Names: TH588; TH-588; TH 588. Product Category: Inhibitors. Appearance: Solid powder. CAS No. 1609960-31-7. Molecular formula: C13H12Cl2N4. Mole weight: 295.17. Purity: >98%. IUPACName: N4-cyclopropyl-6-(2,3-dichlorophenyl)pyrimidine-2,4-diamine. Canonical SMILES: NC1=NC(C2=CC=CC(Cl)=C2Cl)=CC(NC3CC3)=N1. Product ID: ACM1609960317. Alfa Chemistry ISO 9001:2015 Certified. Categories: TH 88 (MN). | |
| TH588 | TH588 is first-in-class nudix hydrolase family inhibitor that potently and selectively engage and inhibit the MTH1 (IC50= 5 nM). Uses: Scientific research. Group: Signaling pathways. CAS No. 1609960-31-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12814. | |
| TH588 hydrochloride | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| TH-6 | TH-6 is a potent HDAC inhibitor with IC 50 s of 0.115, 0.135, 0.242, 0.138, 2.120 μM for HDAC1, HDAC2, HDAC3, HDAC6, HDAC8, respectively. TH-6 inhibits cell migration and invasion. TH-6 induces apoptosis and cell cycle arrest at G2/M phase. TH-6 shows anti-tumor activity [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 3031349-25-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-149029. | |
| TH9619 | TH9619 is a potent inhibitor of dehydrogenase and cyclohydrolase activities in both MTHFD1 and MTHFD2 with a IC50 value of 47 nM, and selectively kills cancer cells. TH9619 induces apoptosis by blocking the S phase. TH9619 has antitumor activity[1][2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2379556-22-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-155950. | |
| Thailanstatin A | Thailanstatin A is an ultra-potent inhibitor of eukaryotic RNA splicing (IC50=650 nM). Thailanstatin A exerts effects via non-covalent binding to the SF3b subunit of the U2 snRNA subcomplex of the spliceosome and shows low-nM to sub-nM IC50s against multiple cancer cell lines. Thailanstatin A, a payload for ADCs, is conjugated to the lysines on trastuzumab yielding linker-less ADC[1][2][3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1426953-21-0. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-129589. | |
| Thailanstatin B | Thailanstatin B is a pre-mRNA splicing inhibitor. Thailanstatin B is used as a cytotoxin for ADCs. Synonyms: EX-A5053. CAS No. 1426953-23-2. Molecular formula: C28H42ClNO9. Mole weight: 572.1. |  |
| Thailanstatin C | Thailanstatin C is an antiproliferative agent and pre-mRNA splicing inhibitor (IC50 = 6.84 μM) from Burkholderia thailandensis MSMB43. Synonyms: (1S,5R)-1,5-Anhydro-1-(carboxymethyl)-3-C-(chloromethyl)-2-deoxy-5-{(1E,3E)-5-[(2S,3S,5R,6R)-5-{[(2Z,4S)-4-(isobutyryloxy)-2-pentenoyl]amino}-3,6-dimethyltetrahydro-2H-pyran-2-yl]-3-methyl-1,3-pentadien-1-yl}-D-erythro-pentitol; D-arabino-Heptonic acid, 3,7-anhydro-5-C-(chloromethyl)-2,4-dideoxy-7-C-[(1E,3E)-3-methyl-5-[(2S,3S,5R,6R)-tetrahydro-3,6-dimethyl-5-[[(2Z,4S)-4-(2-methyl-1-oxopropoxy)-1-oxo-2-penten-1-yl]amino]-2H-pyran-2-yl]-1,3-pentadien-1-yl]-, (7R)-. Grade: ≥95%. CAS No. 1426953-24-3. Molecular formula: C30H46ClNO9. Mole weight: 600.14. | |
| Thailanstatin D | Thailanstatin D inhibits AR-V7 gene splicing by interfering the interaction between U2AF65 and SAP155 and preventing them from binding to polypyrimidine tract located between the branch point and the 3' splice site. Thailanstatin D exhibits a potent tumor inhibitory effect on human CRPC xenografts leading to cell apoptosis. Synonyms: Spliceostatin C. CAS No. 1609105-89-6. Molecular formula: C28H41NO8. Mole weight: 519.63. | |
| thalianol synthase | This enzyme belongs to the family of isomerases, specifically those intramolecular transferases transferring other groups. Group: Enzymes. Synonyms: (S)-2,3-epoxysqualene mutase (cyclizing, thalianol-forming). Enzyme Commission Number: EC 5.4.99.31. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-5572; thalianol synthase; EC 5.4.99.31; (S)-2,3-epoxysqualene mutase (cyclizing, thalianol-forming). Cat No: EXWM-5572. |  |
| Thalidomide | Thalidomide inhibits cereblon (CRBN), a part of the cullin-4 E3 ubiquitin ligase complex CUL4-RBX1-DDB1, with a K d of ?250 nM, and has immunomodulatory, anti-inflammatory and anti-angiogenic cancer properties. Thalidomide can work as molecular glue to potentiate substrate. Uses: Scientific research. Group: Signaling pathways. CAS No. 50-35-1. Pack Sizes: 10 mM * 1 mL; 200 mg; 500 mg. Product ID: HY-14658. | |
| Thalidomide (2-(2,6-Dioxo-3-piperidinyl)-1H-iso-indole-1,3(2H)-dione) | Inhibits FGF-induced angiogenesis. Inhibits replication of human immunodeficiency virus type 1. Teratogenic sedative. Group: Biochemicals. Alternative Names: 2-(2,6-Dioxo-3-piperidinyl)-1H-iso-indole-1,3(2H)-dione. Grades: Highly Purified. Pack Sizes: 500mg. US Biological Life Sciences. | Worldwide |
| Thalidomide 4-fluoride | Thalidomide 4-fluoride (Cereblon ligand 4) is the Thalidomide-based Cereblon ligand used in the recruitment of CRBN protein. Thalidomide 4-fluoride (Cereblon ligand 4) can be connected to the ligand for IRAK4 protein by a linker to form PROTAC IRAK4 degrader-1 (HY-129966)[1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cereblon ligand 4; E3 ligase Ligand 4. CAS No. 835616-60-9. Pack Sizes: 1 g; 5 g. Product ID: HY-41547. | |
| Thalidomide-4-O-C4-NH2 hydrochloride | Thalidomide-4-O-C4-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide (HY-14658) based cereblon ligand and a linker used in PROTAC technology. Uses: Scientific research. Group: Signaling pathways. CAS No. 2376990-29-1. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-130948B. | |
| Thalidomide-5-OH | Thalidomide-5-OH is the Thalidomide-based cereblon ligand used in the recruitment of CRBN protein. Thalidomide-5-OH can be connected to the ligand for protein by a linker to form PROTACs[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 64567-60-8. Pack Sizes: 10 mM * 1 mL; 1 g; 5 g; 10 g; 25 g. Product ID: HY-23095. | |
| Thalidomide-5-PEG3-NH2 hydrochloride | Thalidomide-5-PEG3-NH2 is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2761385-81-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-138786A. | |
| Thalidomide-[d4] | Thalidomide-[d4] is the labelled analogue of Thalidomide, which inhibits an E3 ubiquitin ligase and is used as a sedative drug, immunomodulatory agent and also is investigated for treating symptoms of many cancers. Synonyms: Thalidomide D4; 2-(2,6-Dioxo-3-piperidinyl)-1H-iso-indole-1,3(2H)-dione-d4. Grade: 95% by HPLC; 95% atom D. CAS No. 1219177-18-0. Molecular formula: C13H6D4N2O4. Mole weight: 262.25. | |
| Thalidomide-d4 (2-(2,6-Dioxo-3-piperidinyl)-1H-iso-indole-1,3(2H)-dione-d4) | Labelled Thalidomide, which inhibits FGF-induced angiogenesis. Inhibits replication of human immunodeficiency virus type 1. Teratogenic sedative. Group: Biochemicals. Alternative Names: 2-(2,6-Dioxo-3-piperidinyl)-1H-iso-indole-1,3(2H)-dione-d4. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Thalidomide-O-amido-PEG2-C2-NH2 TFA | Thalidomide-O-amido-PEG2-C2-NH2 TFA is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and 2-unit PEG linker used in PROTAC technology. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cereblon Ligand-Linker Conjugates 10 TFA; E3 Ligase Ligand-Linker Conjugates 24 TFA. CAS No. 1957235-75-4. Pack Sizes: 25 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-112617A. | |
| Thalidomide-O-amido-PEG3-C2-NH2 hydrochloride | Thalidomide-O-amido-PEG3-C2-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and 3-unit PEG linker used in PROTAC technology [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2245697-84-9. Pack Sizes: 25 mg; 100 mg. Product ID: HY-107440A. | |
| Thalidomide-O-amido-PEG3-C2-NH2 TFA | Thalidomide-O-amido-PEG3-C2-NH2 TFA is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and 3-unit PEG linker used in PROTAC technology. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cereblon Ligand-Linker Conjugates 3 TFA; E3 ligase Ligand-Linker Conjugates 14 TFA. CAS No. 1957236-21-3. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103611. | |
| Thalidomide-O-C7-acid | Thalidomide-O-C7-acid is a synthetic E3 ligand-linker conjugate containing a cereblon ligand based on Thalidomide and a C7 alkyl linker with a terminal carboxylic acid, as a part of a variety of functionalized PROTAC molecules for binding to a target protein ligand. CAS No. 2169266-70-8. Molecular formula: C21H24N2O7. Mole weight: 416.42. | |
| Thalidomide-O-COOH | Thalidomide-O-COOH is the Thalidomide-based Cereblon ligand used in the recruitment of CRBN protein. Synonyms: E3 ligase Ligand 3; Thalidomide-Acid; Thalidomide-carboxylic acid; 2-((2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-4-yl)oxy)acetic acid; 2-[[2-(2,6-Dioxo-3-piperidinyl)-2,3-dihydro-1,3-dioxo-1H-isoindol-4-yl]oxy]acetic acid. Grade: ≥ 98%. CAS No. 1061605-21-7. Molecular formula: C15H12N2O7. Mole weight: 332.26. | |
| Thalidomide-piperazine hydrochloride | Thalidomide-piperazine hydrochloride has the potential for the research of leprosy and multiple myeloma. Thalidomide-piperazine hydrochloride used as a tool in developmental biology leads to important discoveries in the biochemical pathways of limb development [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2228029-82-9. Pack Sizes: 25 mg; 50 mg. Product ID: HY-132971. | |
| Thalidomide-Piperazine-Piperidine hydrochloride | Thalidomide-Piperazine-Piperidine hydrochloride is a synthesized E3 ligase ligand-linker conjugate. Thalidomide-Piperazine-Piperidine hydrochloride incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2599846-44-1. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-138783A. | |
| Thalidomide-pyrrolidine hydrochloride | Thalidomide-pyrrolidine hydrochloride (compound 18) is an E3 ligase ligand , and can be used for synthesis of PROTACs [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2616553-35-4. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-W248665A. | |
| Thaliporphine | Thaliporphine. Uses: Designed for use in research and industrial production. Additional or Alternative Names: (6aS)-5,6,6a,7-Tetrahydro-2,9,10-trimethoxy-6-methyl-4H-dibenzo[de,g]quinolin-1-ol; Thalicmidine; talikmidine. Product Category: Heterocyclic Organic Compound. CAS No. 5083-88-5. Molecular formula: C20H23NO4. Mole weight: 341.401. Purity: 0.96. IUPACName: THALIPORPHINE. Product ID: ACM5083885. Alfa Chemistry ISO 9001:2015 Certified. | |
| Thalirugidine | Thalirugidine is an alkaloid isolated from the roots of Thalictrum foliolosum. Synonyms: (1S)-1-[[4-[5-[[(1S)-5-hydroxy-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]-2-methoxyphenoxy]phenyl]methyl]-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-5-ol. Grade: 97.0%. CAS No. 64215-95-8. Molecular formula: C39H46N2O8. Mole weight: 670.803. | |
| thallium-201(1+) chloride | thallium-201(1+) chloride. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Thallous chloride tl 201, Thallium-201 chloride, (201-Tl)Thallous chloride, Thallous Chloride, Tl-201, UNII-3I8Y076A0E, Thallous chloride (201TlCl), Thallous chloride tl 201 (TN), MOLI000417, Thallous chloride tl 201 (USP), CID72170, Thallium (201Tl) chloride injection, Thallium (201Tl) chloride injection (JP15), D02402, 55172-29-7. Product Category: Heterocyclic Organic Compound. CAS No. 55172-29-7. Molecular formula: ClTl. Mole weight: 236.424 g/mol. Purity: 0.96. IUPACName: thallium-201(1+) chloride. Product ID: ACM55172297. Alfa Chemistry ISO 9001:2015 Certified. Categories: THALLOUS CHLORIDE TL-201. | |
| Thallium 205Tl (certified for isotope abundance ratio) | certified Reference Material. Group: Certified reference materials (crms). | |
| Thallium Ethoxide Powder | Thallium Ethoxide Powder. Group: other nano materials. CAS No. 20398-06-5. Molecular formula: 249.44 g/ mol. Mole weight: Tl(OC2H5). 98%. |  |
| Thallium (I) Acetate | THALLIUM (I) ACETATE, 99.99% pure, -40 mesh, (Synonym: Thallous Acetate), Formula: TlOOCCH3. CAS No. 563-68-8. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! |  Texas TX |
| Thallium (I) Acetate | Thallium (I) Acetate. CAS No. 563-68-8. Pack Sizes: Gram Quantities: 5 gm, 25 gm. Order Number: 3525. |  www.prochemonline.com |
| Thallium (I) Acetate | THALLIUM (I) ACETATE, 99.9% pure, -60 mesh, (Synonym: Thallous Acetate), Formula: TlOOCCH3. CAS No. 563-68-8. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! | Texas TX |
| Thallium (I) Acetate | THALLIUM (I) ACETATE, 99.999% pure, -60 mesh, (Synonym: Thallous acetate; Acetic Acid, Thallium Salt), Formula: TlOOCCH3. CAS No. 563-68-8. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! | Texas TX |
| Thallium(I) Acetate 99+% | Used in microbiology as a selective growth medium. Group: Biochemicals. Alternative Names: Thallium Acetate; Thallium monoacetate; Thallium(1+) Acetate; Thallium(I) Acetate; Thallous Acetate. Grades: Reagent Grade. CAS No. 563-68-8. Pack Sizes: 5g, 25g, 100g, 250g. Molecular Formula: C2H3O2Tl, Molecular Weight: 263.42. US Biological Life Sciences. | Worldwide |
| Thallium(I) acetate, 99.99% | 5g Pack Size. Group: Building Blocks, Catalysts. Formula: CH3COOTl. CAS No. 563-68-8. Prepack ID 62383102-5g. Molecular Weight 263.43. See USA prepack pricing. |  |
| Thallium(I) acetylacetonate | Thallium(I) acetylacetonate. Group: Solution deposition precursors. Alternative Names: Thallium(I) 2,4-pentanedionate. CAS No. 25955-51-5. Product ID: [(Z)-4-Oxopent-2-en-2-yl]oxythallium. Molecular formula: 303.49. Mole weight: C5H7O2Tl. CC(=CC(=O)C)O[Tl]. InChI=1S/C5H8O2.Tl/c1-4(6)3-5(2)7; /h3, 6H, 1-2H3; /q; +1/p-1/b4-3-. QGQYKYKTENVDSC-LNKPDPKZSA-M. 95%+. | |
| Thallium (I) Bromide | THALLIUM (I) BROMIDE, 99.9% pure, -8 mesh, (Synonym: Thallous Bromide), Formula: TlBr. CAS No. 7789-40-4. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! | Texas TX |
| Thallium (I) Bromide | Thallium (I) Bromide. Grades: 99.% Extremely High (>=99%). CAS No. 7789-40-4. Pack Sizes: Gram Quantities: 25 gm, 100 gm. Order Number: 3529. | www.prochemonline.com |
| Thallium (I) Bromide | THALLIUM (I) BROMIDE, 99.99% pure, -20 mesh, (Synonym: Thallous Bromide), Formula: TlBr. CAS No. 7789-40-4. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! | Texas TX |
| Thallium (I) Carbonate | THALLIUM (I) CARBONATE, 99.9% pure, -40 mesh, (Synonym: Thallous Carbonate), Formula: Tl2CO3. CAS No. 29809-42-5. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! | Texas TX |
| Thallium (I) Carbonate | THALLIUM (I) CARBONATE, 99.999% pure, -20 mesh, (Synonym: Thallous Carbonate), Formula: Tl2CO3. CAS No. 29809-42-5. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! | Texas TX |
| Thallium (I) Carbonate | THALLIUM (I) CARBONATE, 99.99% pure, -30 mesh, (Synonym: Thallous Carbonate), Formula: Tl2CO3. CAS No. 29809-42-5. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! | Texas TX |
| Thallium (I) Chloride | THALLIUM (I) CHLORIDE, 99.9% pure, -20 mesh, (Synonym: Thallous Chloride), Formula: TlCl. CAS No. 7791-12-0. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! | Texas TX |
| Thallium (I) Chloride | THALLIUM (I) CHLORIDE, 99.999% pure, -20 mesh, (Synonym: Thallous Chloride), Formula: TlCl. CAS No. 7791-12-0. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! | Texas TX |
| Thallium(I) cyclopentadienide | Thallium(I) cyclopentadienide. Uses: Designed for use in research and industrial production. Additional or Alternative Names: THALLIUM CYCLOPENTADIENIDE;2,4-cyclopentadien-1-yl-thalliu;2,4-Cyclopentadien-1-ylthallium;2-Cyclopentadienyl thallium;Thallium(I) cyclopentadienide;Thallium, 2,4-cyclopentadien-1-yl-;Thallium, pi-cyclopentadienyl-;Thallous cyclopentadienide. Product Category: Polymer/Macromolecule. CAS No. 34822-90-7. Molecular formula: C5H5Tl 5*. Mole weight: 269.48. Product ID: ACM34822907. Alfa Chemistry ISO 9001:2015 Certified. | |
| Thallium(I) ethoxide | Thallium(I) ethoxide. Group: Solution deposition precursors. Alternative Names: ethanol,thallium(1+)salt; Ethyl alcohol, thallium (I); KS-000018Q5; Thallium (I) ethanolate; Thallous ethoxide; Ethanol, thallium(1+) salt (1:1); DZFYOYRNBGNPJW-UHFFFAOYSA-N; ETHANOL, THALLIUM(1+) SALT; SCHEMBL690956; 20398-06-5. CAS No. 20398-06-5. Product ID: ethanolate; thallium(1+). Molecular formula: 249.441g/mol. Mole weight: C2H5OTl. CC[O-].[Tl+]. InChI=1S/C2H5O.Tl/c1-2-3;/h2H2, 1H3;/q-1;+1. DZFYOYRNBGNPJW-UHFFFAOYSA-N. | |
| Thallium (I) Formate | THALLIUM (I) FORMATE, 99.9% pure, -40 mesh, (Synonym: Thallous Formate), Formula: TlOOCH. CAS No. 992-98-3. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! | Texas TX |
| Thallium(I) hexafluoroacetylacetonate | Thallium(I) hexafluoroacetylacetonate. Group: Solution deposition precursors. CAS No. 15444-43-6. Molecular formula: 411.43. Mole weight: TlC5HF6O2. | |
| Thallium (III) Acetate | Thallium (III) Acetate. CAS No. 2570-63-0. Pack Sizes: Gram Quantities: 10 gm, 50 gm. Order Number: 3526. | www.prochemonline.com |
| Thallium (III) Nitrate | THALLIUM (III) NITRATE, TRIHYDRATE, 99.5% pure, crystalline, Formula: Tl(NO3)3.3H2O. CAS No. 13453-38-8. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! | Texas TX |
| Thallium (III) Nitrate | Thallium (III) Nitrate. Grades: 99.99% Extremely High (>=99%). CAS No. 13453-38-8. Pack Sizes: Gram Quantities: 25 gm, 100 gm. Order Number: 3559. | www.prochemonline.com |
| Thallium (III) Oxide | THALLIUM (III) OXIDE, 99.5% pure, -20 mesh, (Synonym: Thallic Oxide; Thallium Sesquioxide), Formula: Tl2O3. CAS No. 1314-32-5. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! | Texas TX |
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